KONICA MINOLTA DI-X1 - Indonesia BPOM Medical Device Registration

KONICA MINOLTA DI-X1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220188. The device is manufactured by KONICA MINOLTA TECHNOPRODUCTS CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MURSMEDIC.

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BPOM Registered

Risk Class Kelas Resiko : C

KONICA MINOLTA DI-X1

Analysis ID: AKL 21501220188

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

KONICA MINOLTA TECHNOPRODUCTS CO., LTD.

Country of Origin

Japan

Authorized Representative

AR Address

Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat

Registration Date

May 29, 2023

Expiry Date

Jul 14, 2025

Product Type

Diagnostic Radiology Equipment

Medical image management and processing system.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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Image Processing Pro Software

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IMAGE PILOT

Kelas Resiko : C

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